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EC Declaration of Conformity

according to the following guidelines:

2014/30/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 26 February 2014
on harmonizing the laws of the Member States relating to electromagnetic compatibility.
RoHS substance bans (2011/65/EU)
WEEE Waste Electrical and Electronic Equipment (2002/96/EC & 2008/34/EC)

The manufacturer / Distributor / Authorized representative

Mindfield Biosystems Ltd.
Hindenburgring 4
D-48599 Gronau
Germany

WEEE-Reg.-Nr. DE 24465971

hereby declares that the following product:

“Mindfield® eSense Muscle”

follows the provisions of the guidelines identified above and their amendments in force at the time of the declaration.

The following harmonized standards have been applied:

DIN EN 62368-1:2016-05 Equipment for audio and video, information and communication technology – Part 1: Safety requirements

DIN EN 61326-1; VDE 0843-20-1:2013-07 Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 1: General requirements (IEC 61326-1:2012); German version EN 61326-1:2013

DIN EN 61326-2-2; VDE 0843-20-2-2:2013-08 Electrical equipment for measurement, control, and laboratory use – EMC requirements – Part 2: Electrical equipment for measurement, control, and laboratory use Part 2-2: Particular requirements – Test arrangement, operating conditions and performance characteristics for the portable test, measurement and monitoring equipment for use in low-voltage power supply systems (IEC 61326-2-2:2012); German version EN 61326-2-2:2013

Place: Gronau
Date: 05. May 2021

Niko RockensĂĽĂź, Managing Director

The Mindfield eSense must be disposed of as electronic scrap in accordance with legal regulations.
WEEE-Reg.-Nr. DE 24465971
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